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Ranitidine Hydrochloride - 68387-310-30 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 68387-310
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 68387-310
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074467
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Ranitidine Hydrochloride

Package NDC: 68387-310-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-310-30)

NDC Information of Ranitidine Hydrochloride

NDC Code 68387-310-30
Proprietary Name Ranitidine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-310-30)
Product NDC 68387-310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


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